Nucleotide sequences for the detection of enterohaemorrhagic Escherichia coli (EHEC)

ABSTRACT

Nucleic sequences of plasmid origin are isolated from bacteria of the enterohaemorrhagic Escherichia coli group (EHEC) and used for the identification of EHEC(s), especially those possessing the genes encoding the virulence factors enterohaemolysin and intimin, and more particularly the specific detection of serotype O157:H7, and in detection kits.

This is a divisional of Ser. No. 09/674,277, filed, Feb. 13, 2001, which is a 371 of PCT/FR99/01000, filed Apr. 27, 1999, the disclosures of which are incorporated herein by reference.

The subject of the invention is two nucleic sequences of plasmid origin, present in bacteria of the enterohaemorrhagic Escherichia coli group (EHEC), the use of the said sequences for the identification of EHEC(s), especially those possessing the genes encoding the virulence factors, enterohaemolysin and intimin, and more particularly the specific detection of serotype O157:H7. The invention also relates to a method using the said sequences as well as the detection kits containing them.

Bacteria of the EHEC group belong to the verotoxin producing Escherichia coli or VTEC family, responsible for diarrhoeic syndromes whose consequences may be fatal in humans. In particular, EHECs can cause haemorrhagic colitis (HC), and possibly the appearance of major complications such as haemolytic uraemic syndrome (HUS) or thrombopenic thrombotic purpura (Griffin et Tauxe, Epidemiol. Rev. 13, 1991, 60-98).

Accordingly, the effect of these infections on public health is such that it involves increased monitoring of foodstuffs and of rapid detection means, in particular in the case of epidemics.

Several serotypes belonging to the EHEC group have been identified and made responsible for various epidemic foci: O157:H7, O26:H11, O111:NM, O103:H2, O145:NM etc. (Acheson et Keush, ASM News 62, 1996, 302-306). However, it is serotype O157:H7 which has been most frequently isolated.

The traditional methods of detection consist in identifying the bacteria or in detecting the toxins secreted by them. The detection of E. coli O157:H7 is mainly carried out on the basis of serotyping, combined with the test for metabolic properties, comprising the absence of fermentation of sorbitol and/or the absence of β-glucuronidase activities. Moreover, no bacteriological method exists which is specific for the detection of EHECs, but tests which make it possible to orient the diagnosis. In particular, the use of agars supplemented with blood or washed red blood cells make it possible to demonstrate the enterohaemolytic character generally present in EHECs.

In general, the bacteriological and immunological methods relating to the detection of E. coli O157:H7 are long, tedious, relatively expensive and require serological confirmation. Moreover, these methods do not make it possible to establish and identification of E. coli O157:H7 because of cross-reactions with other bacterial genera and species, which makes the interpretation difficult.

The use of nucleic probes has therefore appeared as an alternative to these traditional methods. Great efforts have been made to develop these probes, which are capable of detecting, in a sensitive and specific manner, the EHEC-type E. coli bacteria involved in the HC and/or HUS cases, and for which the most widespread prototype is E. coli O157:H7.

In particular, probes or fragments, allowing the detection of the genes responsible for the virulence of E. coli, also called virulence factors, have been published. However, none of the currently known virulence factors makes it possible, on its own, to identify pathogenic strains of E. coli O157:H7 or of EHECs.

Thus, the use of nucleic probes or fragments for the detection of genes encoding verotoxins (vt1 or st1, vt2 or st2), described by many research groups (Karch et Meyer, J. Clin Microbiol. 27, 1989, 2751-2757; Gannon et al., Appl. Env. Microbiol. 58, 1992, 3809-3815; Begum et al., J. Clin. Microbiol. 31, 1993, 3153-3156; Witham et al., Appl. Env. Microbiol. 62, 1996, 1347-1353), has shown that the genes encoding verotoxins are associated with the pathogenic bacterial strains E. coli O157:H7 and other EHECs, but may also be present in nonpathogenic E. coli strains, or possibly in other bacterial types such as Shigella dysenteriae, Citrobacter freundii, and the like.

Likewise, the adhesion protein called intimin is also involved in the virulence of EHEC-type bacteria. Probes have in particular been selected on the corresponding gene (eae) by Gannon et al. in J. Clin. Microbiol. 31, 1993, 1268-1274, Louie et al. in Epidemiol. Infect. 112, 1994, 449-461 and Meng et al. in Int. J. Food Microbiol. 32, 1996, 103-113. However, although this virulence factor is closely associated with the EHEC group, it is also found in enteropathogenic E. coli (EPEC) comprising serotype O55:H7.

Finally, probes have been selected on a plasmid of 60 MDa, encoding, inter alia, enterohaemolysin, a virulence factor also present in many EHECs (Levine et al., J. Infect. Dis. 156, 1987, 175-182; Schmidt et al., Infect. Immun. 63, 1995, 1055-1061). Thus, U.S. Pat. No. 5,475,098 relates to the nucleic sequences contained in the enterohaemolysin operon, corresponding to the hlyA and hlyB genes and to the hlyA-hlyB intergenic region. The claimed oligonucleotide sequences allow specific detection of the EHECs, but the invention does not make it possible to differentiate E. coli O157:H7 from the other EHECs. Moreover, U.S. Pat. No. 5,652,102 describes a nucleic sequence situated on a restriction fragment derived from the plasmid of 60 MDa. However, the use of oligonucleotides derived from this sequence in a polymerase chain reaction (PCR) does not allow, on its own, the specific identification of serotype O157:H7, and consequently requires the joint use of primers amplifying the genes encoding verotoxins and intimin.

The plasmid p0157, isolated from an E. coli 0157:H7 strain obtained from a clinical sample, has recently been described in its entirety (Makino et al., DNA Research 5, 1998, 1-9). Mapping of the plasmid representing the order of the different genes on the genome of the plasmid indicates the presence of 186 open reading frames (ORF). However, the absence of data on the nucleic sequence (data not available at the time of publishing the article) in no case makes it possible to identify a region of diagnostic interest for the specific detection of E. coli O157:H7.

Recently, patent application WO 97/32045 relates to oligonucleotides selected from a chromosomal sequence obtained by the RAPD (Random Amplified Polymorphic DNA) method, leading to the detection of about 99.5% of E. coli O157:H7, but the claimed nucleic sequences also detect nearly 3% of non-EHEC E. coli, which is not satisfactory in terms of specificity in particular in the agri-foodstuffs sector.

The main disadvantage of all these detection systems therefore consists in the fact that none of them makes it possible to establish clearly and simply the identification of the E. coli O157:H7 serotype. It is indeed very often necessary to combine several amplification and/or detection systems in order to make the result accurate. The protocols used are then difficult to carry out (multiple, simultaneous amplifications) and the results obtained, as regards sensitivity and specificity, are highly dependent, not only on the nucleic targets used, but also on the operating conditions.

However, as was indicated above, this serotype can cause serious syndromes which can lead to death, which implies rapid and reliable means of detection, in particular in case of an epidemic.

The work by the inventors consisted in testing for specific sequences from an E. coli O157:H7 genomic library, allowing the recognition of the principal E. coli serotypes pathogenic for humans, and more particularly O157:H7. The library was screened against enteropathogenic E. coli 055:H7, presumed ancestor of serotype O157:H7, the two genomes being extremely closely related according to the polymorphism analyses carried out by T. Whittam et al. in Infect. Immun. 61, 1993, 1619-1629.

This work made it possible to isolate two nucleic fragments of interest for the detection of EHECs and more particularly for the detection of E. coli O157:H7, comprising the nucleic sequences SEQ ID No. 1 and SEQ ID No. 2, situated on the enterohaemolytic plasmid of 60 MDa. The corresponding clones pDF3 and pDF4 containing these sequences were deposited at the Collection Nationale de Cultures de Microorganismes of Institut Pasteur, respectively under the numbers I-1999 and I-2000, on 26 Mar. 1998.

Surprisingly, a first sequence (SEQ ID No. 1) has been identified which comprises the stable combination of a portion of the insertion sequence IS91 and of the sequence derived from the E. coli O157:H7 katP gene or of a portion thereof, the nucleic chain resulting therefrom, never described elsewhere, being specifically found in E. coli O157:H7.

The katP gene, encoding a catalase-peroxidase, is present on the enterohaemolytic plasmid of E. coli O157:H7 and of numerous EHECs (Brunder et al., Microbiol. 142, 1996, 3305-3315), and the insertion sequence IS91, identified on the α-haemolytic plasmids of E. coli (Zabala et al., J. Bacteriol. 151, 1982, 472-476), has still never been described in E. coli O157:H7 type enterohaemolytic strains.

The identification of a truncated insertion sequence at the level of the IS91-katP junction (absence of the left inverted repeat sequence (IR_(L)) from IS91) also suggests a stable integration of IS91 into this portion of the E. coli O157:H7 genome.

Analysis of the amplified products of a large number of O157:H7 strains of various origins demonstrates the conservation of this nucleotide chain within the O157:H7 serotype.

Indeed, an amplified product of 670 base pairs was observed in all the strains tested (55 E. coli 0157:H7 and 1 E. coli 0157:H—) with the primers SEQ ID No. and SEQ ID No. 4, situated respectively in the sequences IS91 and katP.

Moreover, the data obtained from the AluI and RsaI restriction profiles produced on the amplified products of 5 0157:H7 strains of different origins, as well as the sequence analysis performed on 3 strains, including 2 isolated from epidemics (USA, 1993 and Japan, 1996), showed a perfect conservation, that is to say 100% homology, in the sequence portion analysed (SEQ ID No. 1: positions (nt) 272 to 624).

Furthermore, the stable and conserved nucleotide chain is probably a relatively old recombination event which occurred in E. coli O157:H7 during evolution since strains isolated in different places and periods exhibit this same characteristic.

This sequence therefore represents a preferred target for the specific detection of serotype O157:H7.

A second sequence was characterized (SEQ ID No. 2) on the same plasmid, associated with the presence of the virulence factors enterohaemolysin (ehly) and intimin (eae), characters which are specific to the enterohaemorrhagic E. coli strains, comprising serotype O157:H7. In this regard, this fragment is of epidemiological interest because, unlike the methods already known, which require the use of several molecular systems (Paton and Paton, J. Clin. Microbiol. 36, 1998, 598-602), the use of this sequence for a diagnostic application results in a simplified use and in a more rapid interpretation of the results.

The subject of the present invention is therefore the nucleic sequences SEQ ID No. 1 and SEQ ID No. 2, their complementary sequences, the sequences derived therefrom and the fragments which can be used for the specific detection of EHECs, in a food, clinical, veterinary or environmental sample.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows a nucleic action sequence (SEQ ID NO:1) containing 1489 bp, which exhibits homology with the katP gene of E. coli O157:H7 and with the IS91 of E. coli.

FIG. 2 shows a nucleic acid containing 1181 bp, which exhibits homology with the virK plasmid gene encoding a Shigella flexneri virulence protein.

The subject of the present invention is more particularly a specific sequence for the detection of serotype E. coli O157:H7, comprising the sequence SEQ ID No. 1, a fragment of this sequence or a sequence derived therefrom.

According to the invention, the sequence SEQ ID No. 1 comprises a nucleotide chain resulting from a stable recombination event between the sequence of the katP gene or a portion thereof and a truncated insertion sequence IS91.

According to the present invention, the expression nucleic sequence is understood to mean either the DNA or complementary DNA (cDNA) sequence, or alternatively the corresponding RNA sequence.

The invention also relates to the nucleic sequences derived from SEQ ID No. 1 or SEQ ID No. 2, that is to say the sequences differing by mutation, insertion, deletion and/or substitution of one or more bases but nevertheless hybridizing, under conditions of high stringency, with one of the above-mentioned sequences.

According to the invention, the expression high stringency is understood to mean temperature and ionic strength conditions such that they allow specific hybridization between two complementary nucleic acid fragments and limit the nonspecific attachments (Sambrook et al., Molecular Cloning, Second Edition (1989), 9.47-9.62). The temperature conditions are generally between (T_(m) minus 5° C.) and (T_(m) minus 10° C.) when one of the hybrid sequences is short (about twenty nucleotides), T_(m) being the theoretical melting temperature, defined as being the temperature at which 50% of the paired strands separate.

The expression nucleic sequence derived from SEQ ID No. 1 is also understood to mean, according to the invention, any sequence differing from the latter by mutation, insertion, deletion and/or substitution of one or more bases and comprising a chain for stable recombination between the katP gene and the truncated insertion sequence IS91.

More particularly, the nucleic sequences contain at least 8, preferably 10, or most preferably 14 consecutive nucleotides of the chain of FIG. 1, and comprise the nucleotides from position 400 to position 407.

The subject of the present invention is also a second sequence, specific for EHECs, which is SEQ ID No. 2, the sequences complementary thereto, the fragments thereof and the sequences derived therefrom, these sequences being always detected in EHECs, in particular in EHECs jointly possessing the genes encoding enterohaemolysin (ehly) and intimin (eae); said sequence SEQ ID No. 2 being represented in FIG. 2.

The invention also relates to oligonucleotide fragments derived from the sequences SEQ ID No. 1 and SEQ ID No. 2, which can be used as primers in an amplification procedure or as probe in the context of the use of a method of detection, comprising at least 8, advantageously at least 10, more advantageously 14 nucleotides, and preferably up to 30 consecutive nucleotides of the nucleotide chain of SEQ ID No. 1 or SEQ ID No. 2, said primers being capable of hybridizing with the said sequences under high stringency conditions, as defined above.

The primers or probes of the invention also comprise oligonucleotides which can be modified by substitution and/or addition and/or suppression of several nucleotides, or by the addition at one of the ends (generally in 5′ for the primers; 3′ or 5′ for the probes) of a nucleic sequence which is foreign to the desired sequence, or alternatively of a labelling molecule, the said oligonucleotides being nevertheless capable of hybridizing under high stringency conditions with complementary nucleic sequences present in E. coli O157:H7 or in the EHECs.

According to a preferred embodiment of the invention, the oligonucleotides may be used as primers, in a gene amplification procedure, leading to the production of a large quantity of copies of a fragment of SEQ ID No. 1 or of a fragment of SEQ ID No. 2 and allowing respectively the specific detection of E. coli O157:H7 or of the EHECs.

The amplification step may be carried out by any method using conventional methods of enzymatic amplification of DNA or RNA, such as in particular the TAS (Transcription-based Amplification System) technique proposed by Kwoh et al. in PNAS, 86, 1989, 1173-1177, the 3SR (Self-Sustained Sequence Replication) technique described by Fahy et al. in PCR Meth. Appl. 1, 1991, 25-33, the NASBA (Nucleic Acid Sequence-Based Amplification) technique described in patent EP 329 822, or alternatively the SDA (Strand Displacement Amplification) technique described by Walker et al. in P.N.A.S, 89, 1992, 392-396, or advantageously the PCR technique as described in particular in European patents EP 200 362 and EP 201 184 granted in the name of Cetus, or alternatively the techniques derived from the latter and any other method desired for amplifying nucleic sequences in vitro.

In a preferred embodiment of the invention, the oligonucleotides derived from the sequences SEQ ID No. 1 and SEQ ID No. 2 are used in PCR.

The detection of the amplified products may be carried out by gel electrophoresis of all or part of the reaction medium in which the amplification was carried out, in particular on agarose or polyacrylamide gel, or by capillary electrophoresis or chromatography. Visualization of a band of nucleic fragments which is localized at a specific point on the gel makes it possible to assess the size, it being possible for the intensity of this band to be roughly correlated with the number of initial copies of the target to be detected in the sample.

According to another embodiment of the invention, the oligonucleotides, as defined above, may be used as probes in a hybridization procedure for the direct detection of a target nucleic sequence or, after amplification, for the detection of the amplified products.

By way of illustration, the nucleotide fragments may be labelled with a radioactive element (for example ³²P, ³⁵S, ³⁵H, ¹²⁵I) or with a nonradioactive molecule, in particular biotin, acetylaminofluorene, fluorochrome, digoxigenin, or with an enzymatic molecule, or a hapten. Examples of nonradioactive labellings of probes are described, for example, in French patent by P. Kourilsky No. 78.10975, or by M. S. Urdea et al., Nucleic Acids Symp. Ser., 24. 1991, 197-200, or alternatively by R. Sanchez-Pescador, J. Clin. Microbiol. 26, 1988, 1934-1938.

The most general hybridization method consists in immobilizing the nucleic acid extracted from the sample to be analysed on a support (nitrocellulose, nylon, polystyrene and the like) and in incubating the immobilized nucleic acid with the probe under defined temperature and ionic strength conditions. After hybridization, the excess probe is removed and the hybridized molecules formed are detected by the appropriate method (measurement of the radioactivity, of the fluorescence or of the enzymatic activity linked to the probe).

The hybrid molecules formed may also be detected without it being necessary to separate the “bound” and “unbound” phases. It is then said that the detection is carried out in a homogeneous phase. These methods, as described by T. Walker et al. Clin. Chemistry 42, 1996, 9-13 and L. Morrison (Nonisotopic DNA Probe Techniques, Academic Press, 1992, 312-352) relate in particular to fluorescence polarization, in which a probe is labelled with fluoroescein and where the hybridization causes modification of fluorescence, or alternatively the transfer of energy. In the latter case, the detection is based on inter- or intramolecular interactions between two markers. A first marker called “donor” is excited by absorption of light at a particular wavelength. The energy is transferred to a second marker called “acceptor”, which in turn is excited and emits energy.

The oligonucleotide probes may also be used in a detection device comprising an array arrangement of oligonucleotides in which oligonucleotides of a given length are attached in a predetermined order onto a support and overlap with each other by one or more bases; each oligonucleotide being complementary to a DNA or RNA sequence of the target sequence to be detected. The target sequence, which is advantageously labelled, is brought into contact with the array device and can hybridize with the probes attached to the support. An enzymatic treatment then makes it possible to eliminate the incomplete hybrids. Knowing the sequence of a probe at a determined position of the array, it is thus possible to deduce the nucleotide sequence of the target sequence analysed and to deduce the possible mutations which have occurred.

An alternative to the use of a labelled sequence may consist of the use of a support allowing a “bioelectronic” detection of the hybridization of the target sequence with the probes attached onto the support of a material, such as gold, capable of acting, for example, as electron donor at the positions of the array in which a hybrid is formed. The detection of the target nucleic sequence is then determined by an electronic device. An exemplary embodiment of a biosensor is described in patent application EP-0721 016 in the name of Affymax Technologies.

According to a simple and advantageous embodiment, the nucleic probes may be used as capture probes. In this case, the probe termed “capture probe” is immobilized on a support and serves to capture, by specific hybridization, the target nucleic acid from the sample to be tested. If necessary, the solid support is separated from the sample and the duplex formed between the capture probe and the target nucleic acid sequence is then detected by means of a second probe termed “detection probe”, labelled with a detectable element. Advantageously, the capture and detection probes are complementary to two different regions inside the target sequence (amplified or otherwise) to be detected.

The attachment of the capture probe onto the solid support may be made according to methods well known to a person skilled in the art, in particular by passive adsorption or by covalent coupling (Cook et al., Nucleic Acids Res. 16, 1988, 4077-4095; Nagata et al., FEBS Lett. 183, 1985, 379-382; M. Longlaru et al., EP 420 260 A2; T. Gingeras et al., EP 276 302; E Hornes and L. M Kornes, EP 446 260).

The hybridization of the capture and detection probes may occur separately (in two stages) or simultaneously (at the same time), in particular according to one of the methods described by Langhale and Malcolm, Gene 36, 1985, 201-210 or by Ranki et al, Gene 21, 1993, 77-85, by Dunn and Hassel, Cell, 12, 1977, 23-36 or alternatively by Ranki and Soderlund in U.S. Pat. No. 4,486,539 and U.S. Pat. No. 4,563,419.

The subject of the present application is therefore also oligonucleotides derived from SEQ ID No. 1 or from SEQ ID No. 2, selected as primers or probes, capable of hybridizing, under stringent conditions, with a target nucleic acid sequence contained in the tested sample, specific for E. coli O157:H7 or EHECs.

The expression target nucleic sequence is understood to mean any DNA or cDNA or RNA molecule capable of hybridizing under high stringency conditions with an oligonucleotide according to the invention.

The preferred oligonucleotides whose sequences are specified in the annex correspond to the positions on the sequences SEQ ID No. 1 and SEQ ID No. 2 reported in the table below:

Position in Sequence SEQ ID No. 1 SEQ ID No. 3:  9-30 SEQ ID No. 4: 679-658 SEQ ID No. 5:  6-30 SEQ ID No. 6: 682-658 SEQ ID No. 7: 241-263 SEQ ID No. 8: 47-69 SEQ ID No. 9: 251-274 SEQ ID No. 10: 426-401 SEQ ID No. 11: 427-402 SEQ ID No. 12: 391-421 SEQ ID No. 13: 387-417 SEQ ID No. 14: 291-321 SEQ ID No. 15: 510-540 SEQ ID No. 16: 331-350 SEQ ID No. 17: 68-87 SEQ ID No. 18: 397-410 SEQ ID No. 19: 396-411 SEQ ID No. 20: 395-412 SEQ ID No. 21: 718-739 SEQ ID No. 22: 1099 1078 SEQ ID No. 23: 41-60 SEQ ID No. 24: 884-863 SEQ ID No. 25: 928-958 SEQ ID No. 26:  970-1000 SEQ ID No. 27: 883-903

The invention also relates to oligonucleotide pairs, as described above, which can be used as primers for the amplification of a target nucleic sequence corresponding to SEQ ID No. 1 or SEQ ID No. 2, contained in the genome of E. coli O157:H7 or of the EHECs:

The preferred pairs of primers are the following:

for the amplification of E. coli O157:H7:

-   -   SEQ ID No. 3 and SEQ ID No. 4     -   SEQ ID No. 5 and SEQ ID No. 6     -   SEQ ID No. 6 and SEQ ID No. 7     -   SEQ ID No. 6 and SEQ ID No. 8     -   SEQ ID No. 6 and SEQ ID No. 9

for amplification of the EHECs:

-   -   SEQ ID No. 21 and SEQ ID No. 22     -   SEQ No. 23 and SEQ ID No. 24

Thus, the use of the pair of primers SEQ ID No. 5 and SEQ ID No. 6 for carrying out the amplification of the nucleic acid of E. coli O157:H7 leads to the amplification of a nucleic fragment of 676 bp, characteristic of the E. coli O157:H7 strains. The specificity of this fragment may be controlled, where appropriate, by the use of the probe SEQ ID No. 18.

Likewise, the use of the pair of primers SEQ ID No. 21 and SEQ ID No. 22 specifically amplifies a nucleic sequence of 382 bp, present in EHECs, which also possesses the enterohaemolysin and intimin characters. The bacteria belonging to the other E. coli groups, such as the ETECs (enterotoxin-producing E. coli), the EPECs and the like, are not detected. The specificity of the amplified product can moreover be confirmed with the aid of oligonucleotide probes internal to the amplified fragment, such as SEQ ID No. 27.

The subject of the present invention is also oligonucleotides, as described above, which can be used as probes for the detection of an optionally amplified nucleotide sequence. For example, the oligonucleotide sequences SEQ ID No. 14, SEQ ID No. 15 and SEQ ID No. 18 may be used for the specific detection of E. coli O157:H7. Likewise, the use of the sequences SEQ ID No. 25, SEQ ID No. 26 and SEQ ID No. 27 allows the detection of EHECs including O157:H7.

The subject of the invention is also the plasmids containing the sequences SEQ ID No. 1 and SEQ ID No. 2 mentioned above as well as the host cells containing them.

The invention also relates to a method for the in vitro detection of E. coli O157:H7 or EHECs in a sample, characterized in that it comprises the following steps:

1. bringing the sample into contact with one of the pairs of primers, as described above, the nucleic acid contained in the sample having been, where appropriate, made accessible to the hybridization of the primers with the nucleic acid of the target tested for,

2. amplifying the nucleic sequence flanked by the pair of primers chosen,

3. it being possible to carry out the verification of the possible presence of the amplified product according to a method known to persons skilled in the art, as described above.

According to an advantageous embodiment, the amplified fragments may be detected according to the principle of the so-called “sandwich” method.

Also falling within the scope of the invention is a method for the in vitro detection of previously amplified nucleotide sequences specific for E. coli O157:H7 or EHECs, by detection on a support, for example a microtiter plate and, characterized in that it comprises the following steps:

-   -   denaturation of the amplified sequence of E. coli O157:H7 and/or         EHECs by a physical or chemical means. The addition of a         denaturing solution composed of 200 mM NaOH, 40 mM EDTA will be         preferred,     -   bringing denatured amplified fragments into contact, in an         appropriate hybridization buffer, with, on the one hand, at         least one capture probe attached to the support, and on the         other hand, at least one free detection nucleic probe in the         hybridization buffer, optionally labelled, capable of         hybridizing with the same strand of the amplified fragments as         that with which the capture probe is hybridized, but in a region         different from that hybridized with the capture probe; it being         possible for the said hybridization solution to be         advantageously 5-fold concentrated SSPE (Sodium Saline Phosphate         EDTA; Molecular Cloning, A practical guide, Sambrook et al.,         Vol. 3, 1989, annexe B13), 0.5% Tween 20, 0.01% Merthiolate,     -   incubation of the reaction mixture for a sufficiently long         period to allow the hybridization; it being possible for this         incubation, for example, to be advantageously performed at         37° C. for about 1 hour,     -   one or more washings of the preceding mixture, in order to         remove any unreacted nucleic sequence; it being possible for the         said washings, for example, to be carried out with a solution         containing 10 mM Tris-HCl, 300 mM NaCl and 0.1% Tween 20, pH         7.4,     -   visualization of the detection probes hybridized with the         amplified nucleic sequences.

According to an advantageous embodiment of the invention, the detection probe is labelled with peroxidase, and the activity of the peroxidase linked to the hybridized detection probe is visualized by colorimetric reading, in the presence of a chromogenic substrate, according to the following steps:

-   -   deposition of a solution containing a chromogenic substrate,         such as tetramethylbenzidine (TMB), in each of the wells         containing the reaction mixture, and incubation, in the dark, of         the microplate for a sufficient period, generally 20 to 30 min,         and then the reaction is stopped by the addition of a blocking         solution, the said solution being advantageously an H₂SO₄         solution used at a final concentration of 0.5 N,     -   determination of the optical density, the said determination         being carried out at a wavelength of 450 nm (reference 620 nm)         when TMB is used as chromogenic substrate.

According to a particularly advantageous embodiment, the capture probe used for the detection of E. coli O157:H7 may be SEQ ID No. 15 and the detection probe is the oligonucleotide SEQ ID No. 18. Likewise, the capture probe used for the detection of EHEC bacteria may be SEQ ID No. 25 and the detection probe of the oligonucleotide SEQ ID No. 27.

The invention also relates to a detection kit, for the identification of E. coli O157:H7 or EHECs, contained in a sample, comprising among the reagents:

-   -   at least two oligonucleotides as defined above, used as primers         for the amplification of E. coli O157:H7 or of the bacteria of         the EHEC group,     -   optionally, a component for verifying the sequence of the         amplified fragment, more particularly a nucleic probe as defined         above.

The following examples are given without limitation to illustrate the invention.

EXAMPLE 1 Characterization of the Sequences SEQ ID No. 1 and SEQ ID No. 2

1) Construction of the E. Coli O157:H7 Genomic Library:

The genomic DNA for the E. coli O157:H7 strain isolated from stools from a patient suffering from haemorrhagic colitis and producing type 1 and 2 verotoxins was partially digested with the endonuclease Pstl (Boehringer Mannheim, Ref. 621625) by allowing 0.03 enzyme unit to act per μg of DNA in buffered medium for 1 hour at 37° C. The genomic DNA thus digested made it possible to generate fragments of 35-45 kb. The cosmid pHC79 (Hohn and Murray, Proc. Natl. Acad, Sci 74, 1977, 3259-3263) was digested in the same manner and dephosphorylated so as to avoid any self-ligation.

The ligation was carried out by mixing 900 ng of vector and 2.6 μg of DNA fragments of 35-45 kb (that is a vector/insert molar ratio of 2), the reaction medium being left at 14° C. for 18 hours after having been supplemented with 2 units of T4 DNA ligase (Boehringer Mannheim; Ref. 481220). The recombinant cosmids were encapsidated in vitro and used to transform the E. coli XL1-Blue MR bacteria (Stratagene; Ref. 200300). The transformed bacteria were incubated for 1 hour at 37° C. in LB medium (Luria-Bertani, Molecular Cloning, A practical guide, Sambrook et al., Vol. 3, 1989, annexe A1). The DNA fragments of 35-45 kb being inserted into the vector pHC79 so as to abolish the ampicillin resistance site and to conserve the tetracycline resistance site, the bacteria were then plated on selective agar medium containing 12.5 μg/ml of tetracycline.

Mini preparations of cosmid DNA were produced from the first 360 colonies isolated on tetracycline using the REAL Prep96 Kit distributed by Quiagen (reference 26171).

The DNA of these preparation was then digested with the endonucleases Pstl, EcoRI and Sall (Boehringer Mannheim, Ref. 621625, 703737 and 567663), analysed by electrophoresis on 1.2% agarose gel and then transferred onto Hybond N⁺ nylon filter (Amersham, Ref. RPN 303B). The DNA was irreversibly fixed by exposure to UV for 5 min.

2) Screening of the Library:

The hybridizations were carried out with a homologous DNA probe obtained from the E. coli O157:H7 strain (Collection de l'Institut Pasteur, No. 103571) and with a heterologous DNA probe consisting of a “pool” of DNA obtained from 8 E. coli 055:H7 strains (Collection de l'Institut Pasteur, No. 105215, 105216, 105217, 105228, 105239, 105240, 105241, 105242).

The various filters were hybridized for 16 to hours at 65° C. in a solution containing 6-fold concentrated SSC buffer (Sodium Saline Citrate; Molecular Cloning, A practical guide, Sambrook et al., Vol. 3, 1989, annexe B13), 5-fold concentrated Denhart's solution (Molecular Cloning, Vol. 3, 1989, annexe B15), 10% Dextran sulphate (Pharmacia Biotech, Ref. 17-0340-02), 10 mM EDTA, 0.5% SDS, 100 μg/ml single-stranded salmon sperm DNA and the relevant DNA (O157:H7).

After hybridization, the filters were washed twice 10 min in a 2-fold concentrated SSC buffer at 65° C., once 30 min in a buffer containing 2-fold concentrated SSC and 0.1% SDS at 65° C. and then once 10 min in SSC diluted 1/10 at 65° C. The filters, which are still wet, were exposed in a cassette with an intensifying screen for 24 to 48 hours at −80° C.

After the necessary exposure time, the films were developed and then the nylon membranes dehybridized by performing 4 to 5 bathing cycles at 45° C., with stirring. For each cycle, two successive baths of 30 min in a 0.5 N NaOH solution and then 30 min in a buffer containing SSC diluted 1/10 and 0.1% SDS were performed. The membranes were finally washed in 2-fold concentrated SSC and placed in a cassette in order to verify that no traces of hybridization remain. After dehybridization, the filters were hybridized in the same manner as above with a pool of nonrelevant DNA (O55:H7).

3) Isolation and cloning of the fragments SEQ ID No. 1 and SEQ ID No. 2:

The results of these hybridizations made it possible to identify two cosmid clones from which one fragment of about 1 to 2 kb, hybridizing with the homologous probe and not hybridizing with the heterologous probe, was isolated respectively. After having verified their conservation in various O157:H7 strains by “dot-blot” hybridization, these fragments were cloned into a vector pUC18 (Oncor Appligene Ref. 161131) and then prepared in a large quantity. The recombinant plasmids were called pDF3 and pDF4 and correspond respectively to the sequences SEQ ID No. 1 and SEQ ID No. 2.

4) Determination of the sequences SEQ ID No. 1 and SEQ ID No. 2

The fragments were sequenced according to the Sanger et al. method described in Proc. Natl. Acad. Sci. 74, 1977, 5463, using the “universal primer” and the “reverse primer” of the plasmid pUC18, as well as oligonucleotides internal to the sequences.

The sequence SEQ ID No. 1 (FIG. 1), containing 1489 bp, exhibits 99.9% homology with the katP gene of E. coli O157:H7 in the region 407 to 1489 and a 95.8% homology with the IS91 of E. coli in the region 1 to 406.

The analysis of the sequence SEQ ID No. 2 (FIG. 2), containing 1181 bp, reveals no known sequence of the enterohaemolytic plasmid. Only the portion 237 to 570 exhibits 68% homology with the virK plasmid gene encoding a Shigella flexneri virulence protein.

EXAMPLE 2 Specific Detection of E. Coli O157:H7

The specificity study was performed on 100 E. coli strains of different serotypes and 42 non-E. coli strains comprising, inter alia, bacteria capable of cross-reacting with E. coli O157:H7 such as for example Salmonella, Shigella dysenteriae, Citrobacter freundii, Hafnia alvei, Escherichia hermanii.

1) Extraction of the DNA:

The DNA sequences are obtained by the method of boiling in the presence of Chelex (InstaGene™ Matrix, Biorad). The samples were prepared according to the following protocol:

A bacterial suspension is produced in sterile ultrapure water from several bacterial colonies isolated on Tryptone-Casein-soybean agar (Sanofi Diagnostics Pasteur, Ref. 53455), and then centrifuged at 10,000-12,000 revolutions/min for 2-3 min and the supernatant carefully removed. The bacterial pellet is resuspended in 200 μl of lysis reagent, homogenized and then incubated in a heating block at 100° C. for 10-15 min. The sample is again homogenized and then centrifuged at 10,000-12,000 revolutions/min for 2-3 min. The DNA can be amplified directly or stored at −20° C.

2) Amplification by PCR:

The amplification reaction is carried out in a total volume of 15 μl containing 50 mM KCl; 10 mM Tris-HCl pH8.3; 0.01% gelatin; 3 mM MgCl₂; 0.25 μM of each primer SEQ ID No. 5 and SEQ ID No. 6; 100 μM (dATP, dCTP, dGTP); 400 μM dUTP; 0.5 unit of Uracyl-DNA-Glycosylase (UDG; BRL Life Technologies); one unit of Taq DNA Polymerase (BRL Life Technologies) and 5 μl of DNA prepared as indicated in paragraph 1.

After incubating at 50° C. for 2 min and then at 95° C. for 5 min, the samples are subjected to 35 amplification cycles composed of 15 sec at 95° C., 15 sec at 65° C. and 15 sec at 72° C. The tubes are kept at 72° C. until the plate is removed.

The thermal cycles are performed in a “Perkin-Elmer 9600” thermocycler.

Each experiment comprises a positive control and a negative control.

3) Visualization of the Amplified Products:

The amplification reactions are visualized on agarose gel or detected on microplate.

3-1) Agarose Gel:

After amplification, 15 μl of chloroform are added to each sample in order to inactivate the UDG and then one aliquot of each reaction is analysed by electrophoresis on 1.2% agarose gel stained with ethidium bromide, in the presence of a size marker. Visualization of a DNA fragment at 676 by indicates the presence of E. coli O157:H7 in the sample tested.

3-2) Hybridization in Microplate:

The amplification products are denatured by addition, volume for volume, of a solution containing 200 mM NaOH, 40 mM EDTA. The microplate, in which the surface of the wells is coated with the capture probe SEQ ID No. 15, is prehybridized in a hybridization buffer containing 5-fold concentrated SSPE, 0.5% Tween 20 and 0.01% Merthiolate. Next, the microplate is emptied and each of the wells receives 200 μl of hybridization buffer containing the denatured amplified fragment and the revealing probe SEQ ID No. 18. The incubation is performed at 37° C., with stirring, for 1 hour.

The wells are then washed six times with 400 μl of solution (10 mM Tris-HCl pH 7.4; 300 mM NaCl and 0.1% Tween 20), and then the activity of the peroxidase bound to the probe is detected by adding to each well 200 μl of a detection solution containing the chromogene tetramethylbenzidine (TMB). The microplate is incubated at 37° C., in the dark, for 30 min and then 100 μl of a 1.5 N H₂SO₄ solution are added in order to block the reactions. The optical density values are determined at 450 nm against a reference at 620 nm.

4) Study of Specificity:

The tests were performed on a total of 142 bacterial strains, using the pair of primers SEQ ID No. 5 and SEQ ID No. 6 for the PCR amplification step, the capture probe SEQ ID No. 15 and the detection probe SEQ ID No. 18 for the hybridization step on microplates.

The results obtained on microplates with the E. coli strains and non-E. coli strains (bacteria of different genera and species) are presented respectively in Tables I and II below:

TABLE I E. coli strain Number of PCR SEQ ID (serotype) strains tested No. 5/6 VTEC/EHEC O157:H7 55 + O157:H- 1 + O26:H11 10 − O111:H- 2 − O145:H- 2 − O103:H2 2 − O121:H19 1 − O165:H25 1 − O45:H2 1 − O22:H8 2 − O137:H41 1 − O91:H21 1 − O141:H4 1 − EPEC O55:H7 8 − O55:H6 1 − O55:H- 1 − O111:H- 1 − O111:H2 1 − O111:H12 1 − O128:H2 1 − O127:H6 1 − ETEC O157:H19 1 − O159:H34 1 − CIP 81.86 1 − E. Coli CIP 76.24 1 − CIP 54.8 1 − The (+) results correspond to OD₄₅₀ > 2.5. The (−) results correspond to OD₄₅₀ < 0.05.

TABLE II Strain Number of PCR SEQ ID (bacterial species) strains tested No. 5/6 Salmonella Salmonella (Groups I to VI) 10 − Shigella Shigella flexneri 2 − Shigella dysenteriae 1 − Shigella sonnei 1 − Others Escherichia hermanii 2 − Citrobacter freundii 2 − Yersinia enterocolitica 2 − Yersinia pseudotuberculosis 1 − Hafnia alvei 1 − Proteus mirabilis 1 − Proteus vulgaris 1 − Serratia marcescens 1 − Klebsiella pneumoniae 2 − Klebsiella oxytoca 1 − Enterobacter cloacae 1 − Enterobacter aerogenes 1 − Enterobacter agglomerans 1 − Bacillus subtilis 1 − Morganella morganii 1 − Providencia alcalifaciens 1 − Vibrio parahaemolyticus 1 − Acinetobacter baumanii 1 − Shewanella putrefaciens 1 − Pseudomonas aeruginosa 1 − Pseudomonas fluorescens 1 − Listeria monocytogenes 3 − The (+) results correspond to OD₄₅₀ > 2.5. The (−) results correspond to OD₄₅₀ < 0.05.

In conclusion, only the O157:H7 and 0157:H-strains are detected on microplates with the abovementioned system.

EXAMPLE 3 Specific Detection of EHECs

The specificity was tested on a total of 142 bacterial strains including various serotypes of E. coli as well as other bacterial species which can interfere with the detection of the EHECs.

The DNAs were extracted according to the protocol described in the first paragraph of Example 2.

The amplification conditions are the following: The reaction is carried out in a total volume of 50 μl containing 50 mM KCl; 10 mM Tris-HCl pH 8.3; 1.5 mM MgCl₂; 0.5 μM of each primer SEQ ID No. 21 and SEQ ID No. 22; 200 μM (dATP, dCTP, dGTP, dTTP); one unit of Taq DNA Polymerase (BRL Life Technologies) and 5 μl of DNA prepared as indicated in paragraph 1 of Example 2.

The thermal cycles are performed in a “Perkin-Elmer 9600” thermocycler.

Each experiment comprises a positive control and a negative control.

The amplification products were visualized on agarose gel stained with EtBr, the presence of a band at 382 by indicating the presence of EHEC in the sample tested.

The results are presented in Table III.

Only the strains exhibiting the ehly and eae characters, virulence factors frequently associated in the strains isolated from human infections, are detected by PCR with the pair of primers SEQ ID No. 21 and SEQ ID No. 22.

Furthermore, the use of the said pair of primers also makes it possible to detect in particular, by means of a single amplification reaction, the E. coli strains possessing the genotype (vt⁺ eae⁺ and ehly⁺), characteristic of the enterohaemorrhagic E. coli.

TABLE III Strain Number of PCR SEQ ID (serotype) strains tested Genotype No. 21/22 VTEC/EHEC O157:H7 54 vt+, ehly+, eae+ + 1 vt−, ehly+, eae+ + O157:H- 1 vt+, ehly+, eae+ + O26:H11 5 vt+, ehly+, eae+ + 1 vt−, ehly+, eae+ + O26:H- 1 vt+, ehly+, eae+ + O111:H- 1 vt+, ehly+, eae+ + O145:H- 2 vt+, ehly+, eae+ + O103:H2 2 vt+, ehly+, eae+ + O121:H19 1 vt+, ehly+, eae+ + O165:H25 1 vt+, ehly+, eae+ + O45:H2 1 vt+, ehly+, eae+ + O22:H8 2 vt+, ehly+, eae− − O137:H41 1 vt+, ehly+, eae− − O91:H21 1 vt+, ehly+, eae− − O26:H11 3 vt+, ehly−, eae+ − O111:H- 1 vt+, ehly−, eae+ − O141:H4 1 vt+, ehly−, eae− − EPEC O55:H7 8 vt−, ehly−, eae+ − O55:H6 1 vt−, ehly−, eae− − O55:H- 1 vt−, ehly−, eae− − O111:H- 1 vt−, ehly−, eae− − O111:H2 1 vt−, ehly−, eae+ − O111:H12 1 vt−, ehly−, eae− − O128:H2 1 vt−, ehly−, eae+ − O127:H6 1 vt−, ehly−, eae+ − ETEC O157:H19 1 vt−, ehly−, eae− − O159:H34 1 vt−, ehly−, eae− − CIP 81.86 1 vt−, ehly−, eae− − E. coli CIP 76.24 1 vt−, ehly−, eae− − CIP 54.8 1 vt−, ehly−, eae− − non-E. coli 42 − 

1-19. (canceled)
 20. A pair of isolated nucleic acids selected from the group consisting of: SEQ ID NO: 3 and SEQ ID NO: 4, SEQ ID NO: 5 and SEQ ID NO: 6, SEQ ID NO: 6 and SEQ ID NO: 7, SEQ ID NO: 6 and SEQ ID NO: 8, SEQ ID NO: 6 and SEQ ID NO: 9, SEQ ID NO: 21 and SEQ ID NO: 22, and SEQ ID NO: 23 and SEQ ID NO:
 24. 21. A method for detecting an enterohaemorrhagic Escherichia Coli (EHEC) in a sample, said method comprising detecting a nucleotide chain of sequence SEQ ID NO: 2 by contacting the sample with a nucleic acid consisting of sequence SEQ ID NO: 2, its complementary sequence, a fragment of SEQ ID NO: 2 of at least 8 consecutive nucleotides, or a sequence derived from SEQ ID NO: 2 by mutation, insertion, deletion, and/or substitution of one or more bases, wherein said derived sequence is a nucleotide chain of at least 8 consecutive nucleotides of SEQ ID NO: 2, and wherein said derived sequence hybridizes with sequence SEQ ID NO: 2 or its complementary sequence by contacting with a hybridization solution of 5-fold concentrated sodium saline phosphate EDTA, 0.5% Tween 20, and 0.01% merthiolate followed by washing with a solution containing 10 mM Tris-HCl, 300 mM NaCl, and 0.1% Tween 20, pH 7.4, the presence of said nucleotide chain being indicative of the presence of an EHEC.
 22. The method according to claim 21, wherein said isolated nucleic acid is selected from the group consisting of SEQ ID NOS: 22-27.
 23. The method according to claim 21, wherein said isolated nucleic acid functions as a primer and/or a probe.
 24. The method according to claim 21, wherein said isolated nucleic acid is detectably labeled.
 25. The method according to claim 21, wherein said isolated nucleic acid is immobilized on a support.
 26. The method according to claim 21, comprising the steps of: (a) bringing the sample into contact with a pair of oligonucleotide primers selected from the group consisting of SEQ ID NO: 21-27, the nucleic acid contained in the sample having been, where appropriate, made accessible to the said primers at the target tested for, (b) amplifying the nucleic sequence flanked by the pair of primers, (c) verifying presence of the amplified product by the use of at least one probe specific for the amplified product.
 27. The method according to claim 26, wherein step (c) comprises the substeps of: (c₁) denaturation of the amplified sequences by physical or chemical means, (c₂) bringing a solution containing the denatured amplified sequences of step (c₁) into contact with at least one capture probe and at least one detection probe, optionally labeled, for a period of time sufficient to allow hybridization of the capture and detection probes with the same strand of the denatured amplified sequences, (c₃) washing at least once in order to remove unreacted denatured amplified sequences, (c₄) visualization of the detection probes hybridized with the denatured amplified sequences.
 28. The method according to claim 27, in which the capture probe is attached to the surface of a well of a microtiter plate.
 29. The method according to claim 27, in which the detection probe is labeled with peroxidase.
 30. The method according to claim 29, wherein detection of activity of the peroxidase linked to a hybridized detection probe is carried out by colorimetric reaction, in the presence of a chromogenic substrate, comprising the steps of: addition of the chromogenic substrate to the wells of the microtiter plate containing the solution of denatured amplified sequences, incubation, in the dark, for a sufficient period of time to allow peroxidase color to develop, stopping the hybridization by addition of a blocking solution, determination of the optical density at an appropriate wavelength.
 31. The method according to claim 27, using the following oligonucleotides: sequences SEQ ID NO: 21 and SEQ ID NO: 22, as primers for the amplification, sequence SEQ ID NO: 25, as capture probe, sequence SEQ ID NO: 27, as detection probe.
 32. A method for detecting E. coli 0157:H7 in a sample, which method comprises detecting a nucleotide chain resulting from the stable combination of at least a portion of the insertion sequence IS91 and at least a portion of the sequence of the katP gene with the aid of an isolated nucleic acid comprising at least eight consecutive nucleotides of the sequence SEQ ID NO: 1, the sequence complementary thereto, or of a sequence derived therefrom, differing by mutation, insertion, deletion, and/or substitution of one or more bases and hybridizing with the sequence SEQ ID NO: 1 or its complementary sequence by contacting with a hybridization solution of 5-fold concentrated sodium saline phosphate EDTA, 0.5% Tween 20, and 0.01% merthiolate followed by washing with a solution containing 10 mM Tris-HCl, 300 mM NaCl and 0.1% Tween 20, pH 7.4, the presence of said nucleotide chain being indicative of the presence of E. coli O157:H7.
 33. The method according to claim 32, wherein the sequence of said isolated nucleic acid is selected from the group consisting of sequence SEQ ID NO: 3-SEQ ID NO:
 20. 34. The method according to claim 32, which further comprises detecting a nucleotide chain of sequence SEQ ID NO: 2 with the aid of a second isolated nucleic acid, the second isolated nucleic acid being a chain of at least eight consecutive nucleotides of SEQ ID NO: 2, the presence of said nucleotide chain being indicative of the presence of a EHEC.
 35. The method according to claim 34, wherein the sequence of said second isolated nucleic acid is selected from the group consisting of: SEQ ID NO: 21: 5′-CCACCTGAACGATAAGCGGAAC-3′ SEQ ID NO: 22: 5′-CACCTTCCTTCCATCCTCAGAC-3′ SEQ ID NO: 23: 5′-ATCCCAGCGCGCTCCAGCTG-3′ SEQ ID NO: 24: 5′-ACCCATGATGGCGCATCTGATG-3′ SEQ ID NO: 25: 5′-ACGTTCTGGTCTTACGGGTGATGTAGGTTTT- 3′ SEQ ID NO: 26: 5′-TAGTGAAGCGGTGACAGCATATCAGACGGCT- 3′ SEQ ID NO: 27: 5′-GTGAGATAGGCACAACAATGA-3′.


36. The method according to claim 32, wherein said isolated nucleic acid is used as a primer and/or a probe.
 37. The method according to claim 32, wherein said isolated nucleic acid is detectably labeled.
 38. The method according to claim 32, wherein said isolated nucleic acid is immobilized on a support.
 39. The method according to claim 32, comprising the steps of: (a) bringing the sample into contact with a pair of oligonucleotide primers selected from the group consisting of sequences SEQ ID NO: 3-SEQ ID NO: 20, such that the nucleic acid in the sample is flanked by the pair of nucleotide primers, the nucleic acid contained in the sample having been, where appropriate, made accessible to the pair of oligonucleotide primers at the target tested for, (b) amplifying the nucleic acid sequence flanked by the pair of oligonucleotide primers to produce an amplified product, (c) verification of the presence of the amplified product by using at least one probe specific for the amplified product.
 40. The method according to claim 39, according to which step (c) comprises the following substeps: (c₁) denaturation of the amplified product sequences into fragments by physical or chemical means, (c₂) (i) bringing a solution containing the fragments of amplified product from step (c₁) into contact with at least one capture probe and at least one detection probe, optionally detectably labeled, the capture and detection probes being capable of hybridizing with the same fragment strand, when present, in the fragments of amplified product, and (ii) maintaining the contact for a period of time sufficient to allow the hybridization reaction, (c₃) washing at least once in order to remove unreacted fragments of amplified product, (c4) visualization of hybridized detection probes.
 41. The method according to claim 40, in which the capture probe is attached to the surface of a well of a microtiter plate.
 42. The method according to claim 40, in which the detection probe is labeled with peroxidase.
 43. The method according to claim 42, wherein detection of peroxidase activity is carried out by colorimetric reaction, in the presence of a chromogenic substrate, comprising the steps of: addition of the chromogenic substrate to the wells of the microtiter plate containing the solution of denatured amplified sequences, incubation, in the dark, for a sufficient period of time to allow peroxidase color to develop, stopping the hybridization by addition of a blocking solution, determination of the optical density at an appropriate wavelength.
 44. The method according to claim 40 wherein: the pair of oligonucleotide primers are sequences SEQ ID NO: 5 and SEQ ID NO: 6, the capture probe is sequence SEQ ID NO: 15, the detection probe is sequence SEQ ID NO:
 18. 45. A kit for detecting EHECs, comprising: at least two oligonucleotides primers selected from the group consisting of: SEQ ID NO: 21: 5′-CCACCTGAACGATAAGCGGAAC-3′ SEQ ID NO: 22: 5′-CACCTTCCTTCCATCCTCAGAC-3′ SEQ ID NO: 23: 5′-ATCCCAGCGCGCTCCAGCTG-3′ SEQ ID NO: 24: 5′-ACCCATGATGGCGCATCTGATG-3′ SEQ ID NO: 25: 5′-ACGTTCTGGTCTTACGGGTGATGTAGGTTTT- 3′ SEQ ID NO: 26: 5′-TAGTGAAGCGGTGACAGCATATCAGACGGCT- 3′ SEQ ID NO: 27 5′-GTGAGATAGGCACAACAATGA-3′

optionally at least one oligonucleotide probe selected from the group consisting of: SEQ ID NO: 21: 5′-CCACCTGAACGATAAGCGGAAC-3′ SEQ ID NO: 22: 5′-CACCTTCCTTCCATCCTCAGAC-3′ SEQ ID NO: 23: 5′-ATCCCAGCGCGCTCCAGCTG-3′ SEQ ID NO: 24: 5′-ACCCATGATGGCGCATCTGATG-3′ SEQ ID NO: 25: 5′-ACGTTCTGGTCTTACGGGTGATGTAGGTTTT- 3′ SEQ ID NO: 26: 5′-TAGTGAAGCGGTGACAGCATATCAGACGGCT- 3′ SEQ ID NO: 27: 5′-GTGAGATAGGCACAACAATGA-3′.


46. The kit according to claim 45, comprising: two oligonucleotides of sequences SEQ ID NO: 21 and SEQ ID NO: 22, as a pair of primers, and two oligonucleotides of sequences SEQ ID NO: 25 and SEQ ID NO: 27, for detection.
 47. A Kit for detecting E. coli 0157:H7, comprising: at least two oligonucleotide primers selected from the group consisting of sequences SEQ ID NO: 3-SEQ ID NO: 20; and, optionally, at least one oligonucleotide probe selected from the group consisting of sequences SEQ ID NO: 3-SEQ ID NO:
 20. 48. The kit according to claim 47, comprising: two oligonucleotides of sequences SEQ ID NO: 5 and SEQ ID NO: 6, as a pair of primers, two oligonucleotide of sequences SEQ ID NO: 15 and SEQ ID NO: 18, for detection.
 49. The method of claim 30, wherein the chromogenic substrate is tetramethylbenzidine (TMB).
 50. The method of claim 43, wherein the chromogenic substrate is TMB. 